Keywords:
Angiogenesis; Angiopoietin-1*; metabolism; Arachidonic Acid; metabolism; Arginine; biomarkers; Neonatal Sepsis; Neovascularization
Abstract:
Neonatal sepsis is a major cause of childhood mortality. Limited diagnostic tools and mechanistic insights have hampered our abilities to develop prophylactic or therapeutic interventions. Biomarkers in human neonatal sepsis have been repeatedly identified as associated with dysregulation of angiopoietin signaling and altered arachidonic acid metabolism.